A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036601



Internal ID21945944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75409710..75409820hg38UCSC Ensembl
chr12:75803490..75803600hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605511
Samples
Known GenesGLIPR1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036601
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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